EP0410881A2 - Analogues semi-synthétiques de gangliosides - Google Patents

Analogues semi-synthétiques de gangliosides Download PDF

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EP0410881A2
EP0410881A2 EP90402139A EP90402139A EP0410881A2 EP 0410881 A2 EP0410881 A2 EP 0410881A2 EP 90402139 A EP90402139 A EP 90402139A EP 90402139 A EP90402139 A EP 90402139A EP 0410881 A2 EP0410881 A2 EP 0410881A2
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lyso
acyl
acid
carbon atoms
groups
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Francesco Della Valle
Aurelio Romeo
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Fidia SpA
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    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C07H15/10Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical containing unsaturated carbon-to-carbon bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention concerns semisynthetic ganglioside analogues and more precisely N-acyl-­N,N′-di-lysogangliosides, in which the acyl groups are derived from unsubstituted aliphatic acids having from 1 to 11 carbon atoms, N′-acyl-N,N′-di-lyso-gangliosides and N,N′-diacyl-N,N′-di-lyso-gangliosides, in which the acyl groups are derived from unsubstituted aliphatic acids having from 1 to 24 carbon atoms, but only from 1 to 11 carbon atoms on the sphingosine nitrogen in the case of diacyl derivatives in which the N′-acyl group is acetyl, and functional derivatives of these compounds and the salts of all these compounds.
  • Gangliosides are generally mixtures of various unitary chemical compounds, identifiable by an approximate formula of the following kind: including an oligosaccharide part, generally well-­defined chemically for each ganglioside, a sialic part (i.e. constituted by one or more sialic acids) and a ceramide part, the last three parts generally being constituted by a mixture of various sialic acids and various ceramide residues.
  • oligosaccharide part generally well-­defined chemically for each ganglioside
  • a sialic part i.e. constituted by one or more sialic acids
  • ceramide part the last three parts generally being constituted by a mixture of various sialic acids and various ceramide residues.
  • Sialic acids are acylated derivatives of neuraminic acid with the following formula: in which the amino group is acylated with acetic or glycolic acid and wherein the hydroxyl groups may also be esterified with these acids.
  • sialic and ceramide residues in gangliosides are mixtures of groups with the above formulae and this is also true of the purified gangliosides described in the literature.
  • the number of sialic acids present in gangliosides usually varies between 1 and 5.
  • the sialic residues are bound to the oligosaccharide by a ketose bond formed by the hydroxyl in the 2-position with a hydroxyl of the oligosaccharide.
  • sialic acids of gangliosides are mixtures of various chemically unitary acids, for example N-acetylneuraminic and N-glycolylneuraminic acids, in which the former is predominant, and optionally of one or more of their O-acyl derivatives, for example 8-O-acyl derivatives.
  • Oligosaccharides are composed of a maximum of 5 monosaccharides or their derivatives with an acylamino group, especially hexoses and their derivatives of the aforesaid type. At least one glucose or galactose molecule is always present in the oligosaccharide; the most frequent residues as acylamino derivatives of the aforesaid sugars are N-acetylglucosamine and N-acetylgalactosamine.
  • lysoganglioside is used in the literature to describe compounds derived from natural gangliosides by the elimination of the acyl group present on the sphingosine nitrogen. This elimination can be effected enzymatically, for example by exposing the gangliosides to the action of glycosphingolipid-ceramide-deacylase enzyme. By using this type of hydrolysis it is possible to leave intact the acylamino and acylhydroxyl groups of neuraminic acid. To deacylate these groups also and thus obtain a ganglioside derivative containing two free amino groups, both on the sphingosine nitrogen and on the neuraminic nitrogen, chemical hydrolysis must be used, for example with dilute potassium hydroxide.
  • ganglioside derivatives obtained by deacylation on the neuraminic nitrogen as previously described are usually described in the literature as "de-N-acetyl-­gangliosides", since the acyl group in this position is mainly the acetyl group.
  • N′-lysoganglioside By naming the two nitrogen atoms in the sphingosine and neuraminic residues N and N′ respectively, the nomenclature "N′-lysoganglioside" can be used for the aforesaid de-N-acetyl-gangliosides, in the same way as the term lysogangliosides is used for derivatives with a free amino group in the sphingosine residue, which should therefore be more precisely identified as "N-lysogangliosides".
  • N,N′-di-lyso-gangliosides refers to the compound with both free amino groups. As already noted above, this nomenclature will be used in the present application.
  • the aforesaid definition of derivatives according to the invention encompasses the group of ganglioside derivatives presenting an acetyl group on the neuraminic nitrogen and a C1 ⁇ 11 acyl on the sphingosine nitrogen.
  • the invention also encompasses N-acyl-lyso­gangliosides of this type derived from the aforesaid lysogangliosides obtained enzymatically and with, therefore, acyl groups in the sialic acids as present in natural gangliosides, and that is, mixtures of acylamino groups derived mostly from acetic acid and to a lesser degree from glycolic acid, and optionally with acyl groups esterifying the hydroxy groups.
  • N-lysogangliosides or “N-acyl-lysogangliosides” will therefore be used in the following description of the invention both for these derivatives, which will be qualified as “natural” (for example, natural N-lyso GM1), and for those with a unitary acetyl group on the neuraminic nitrogen, which will be named without this addition, or preferably as a derivative of N,N′-di-lysogangliosides, for example N,N′-di-acetyl-N,N′-di-lyso GM3.
  • acyl-­di-lysogangliosides will however be used hereafter also to signify all the new compounds of the invention.
  • acylation of the amino group of the neuraminic residue with a different acyl from the acetyl (and glycolyl) produces N,N′-diacyl-N,N′-di-lysogangliosides which conserve a natural part of gangliosides, that is the mixed acyl group derived from higher aliphatic acids.
  • N′-acyl-N′-lysogangliosides for example N′-propionyl-N′-lyso GM1, N′-pivaloyl-N′-lyso Gm3, N′-stearoyl-N′-lyso GM1, etc.
  • the new compounds of the present invention are semisynthetic ganglioside analogues differing from gangliosides on account of the presence of unitary and well-defined acyl groups on the sphingosine and/or neuraminic nitrogen (with the exception of natural N-acyl-N-lysogangliosides and N′-acyl-N′-­lysogangliosides) and the fact that the acyl groups are present in different combinations from those observed in natural products.
  • the acyl groups derive from lower homologues of the fatty acids present in natural products, such as stearic acid, with a maximum of 11 carbon atoms and may also have branched chains.
  • those derivatives with an acyl group other than acetyl on the neuraminic nitrogen there may be acyl groups of the aforesaid type on the sphingosine nitrogen or acyls derived from the higher acids typical of natural gangliosides and also homologues with higher molecular weights and up to 24 carbon atoms.
  • derivatives with free amino groups in their sialic parts there are also lower homologues of "natural" acyls on the sphingosine nitrogen.
  • acyl-lysogangliosides of the invention are new substances.
  • Some N-acyl-lysoganglioside derivatives have been described which are included in the aforesaid definition, and more precisely: - N,N′-diacetyl-N,N′-di-lyso GM1 (cf.
  • N-acetyl-N,N′-di-lyso GM3 (Carbohydrate Research 179, 393-410, 1988), - N′-acetyl-N,N′-di-lyso GM3 (Carbohydrate Research 179, 393-410, 1988), - N,N′-diacetyl-N,N′-di-lyso Gm3 (Carbohydrate Research 179, 393-410, 1988).
  • these compounds possess the same or analogous pharmacological actions as described hereafter for the new compounds.
  • This application therefore contains claims to the therapeutic use of such substances as well as the pharmaceutical preparations which contain them as active ingredient.
  • the invention also includes the functional derivatives of the sialic carboxy groups of the new acyl-lysogangliosides, that is, esters and amides and also inner esters with lactone bonds between the sialic carboxy groups and the hydroxyls of the oligosaccharide, analogous to those of gangliosides which are already known, as well as the derivatives peracylated on the ganglioside hydroxyls, both of acyl-lysogangliosides and of their aforesaid functional derivatives, and the salts of all the new acyl-di-lysogangliosides and of their functional derivatives.
  • the functional derivatives of the sialic carboxy groups of the new acyl-lysogangliosides that is, esters and amides and also inner esters with lactone bonds between the sialic carboxy groups and the hydroxyls of the oligosaccharide, analogous to those of gangliosides which are already
  • the main object of the present invention is therefore, more precisely, semisynthetic ganglioside analogues constituted by N-acyl-N,N′-di-lyso­gangliosides, in which the acyl groups are derived from unsubstituted aliphatic acids with from 1 to 11 carbon atoms, by N′-acyl-N,N′-di-lysogangliosides and N,N′-diacyl-N,N′-di-lysogangliosides, in which the acyl groups are derived from unsubstituted aliphatic acids with from 1 to 24 carbon atoms, but with only 1 to 11 carbon atoms in the case of diacyl derivatives in which the N′-acyl group is acetyl, by the esters and/or amides of their sialic carboxy groups and/or by their inner esters and/or by their peracylated derivatives, and optionally by their metal salts either with organic bases or
  • compositions containing one or more of the aforesaid compounds or their mixtures, and/or the corresponding salts, and by pharmaceutical preparations containing as active compound one of the products already described in the literature, or an N-acyl-N,N′-di-lysoganglioside in which the acyl groups are derived from unsubstituted aliphatic acids having from 12 to 24 carbon atoms.
  • a third object is the therapeutic use of the new semisynthetic ganglioside analogues and their aforesaid derivatives, and the use of the aforesaid known products and the aforesaid N-acyl-C12 ⁇ 24-N,N′-di-lysogangliosides.
  • a fourth object of the invention is directed to the manufacturing procedures for all of the new aforesaid semisynthetic ganglioside analogues.
  • the lysogangliosides which serve as a base for the preparation of the new N-acyl derivatives according to the present invention are primarily those which can be obtained by deacylation of gangliosides extractable from natural products, and particularly from tissues of the central or peripheral nervous systems of vertebrates, and also from adrenal marrow, from erythrocytes, from the spleen or other organs. They may be purified gangliosides, as defined in the literature, i.e. those which have a unitary structure in their saccharide part, or they may be ganglioside mixtures.
  • ganglioside group A N-acetylglucosamine and N-acetylgalactoseamine
  • the gangliosides in this group are for example those extracted from vertebrate brain, such as those described in the article "Gangliosides of the Nervous System” in “Glycolipid Methodology", Lloyd A. Witting Ed., American Oil Chemists Society, Champaign, Ill.
  • Glc stands for glucose
  • GalNAC stands for N-acetylgalactosamine
  • Gal stands for galactose
  • NANA stands for N-acetylneuraminic acid.
  • gangliosides of the aforesaid formula I which is substantially the same as for the derivatives of the present invention, and in particular the character of the bond between the saccharide parts, the sialic acids and the ceramide, the following constitutes the complete formula of a "pure" ganglioside GM1 containing one single sialic acid (represented by N-acetylneuraminic or N-glycolylneuraminic acid).
  • the same formula is valid also for a derivative of ganglioside GM1 according to the present invention, with the ceramide residue substituted with a corresponding "artificial" ceramide, in which the N-acyl group is derived from one of the aliphatic acids mentioned previously and/or hereafter, and in which optionally the acetyl group is substituted on the neuraminic nitrogen by one of the acids included in the aforesaid definition of the new compounds.
  • the N-acyl part of the ganglioside mixtures is substituted with one of the aforesaid acyl groups, and these can be obtained by the procedure of the present invention reported hereafter for the deacylation of these ganglioside mixtures and their subsequent reacylation, optionally, after the reacylation of other deacylated groups in the sialic part of the gangliosides.
  • ganglioside extracts obtained from the nervcus system, in particular from the brain and containing gangliosides GM1, GD 1a , GD 1b and GT 1b already mentioned.
  • gangliosides play an important role in the nervous system and it has recently been demonstrated that they are useful in therapy for pathologies of the peripheral and central nervous systems [Acta Psychiat. Scand., 55, 102, (1977); Eur. Medicophys., 13, 1, (1977); Ric. Sci. Educ. Perm. Suppl. 9, 115, (1978); Adv. Exp. Med. Biol. 71, 275, (1976); Electromyogr. Clin. Neurophysiol., 19, 353, (1979); Minerva Medica, 69, 3277, (1978); Minerva Stomat., 27, 177, (1978); Med. del Lavoro, 68, 296 (1977); Brain Res.
  • Ganglioside-stimulated neuronal sprouting enhances functional recovery of damaged nerve tissue.
  • “Outer” esters of gangliosides also present an improved activity on neuronal sprouting and conduction of nerve stimuli, that is, esters of the carboxy function of sialic acids with various alcohols of the aliphatic, araliphatic, alicyclic and heterocyclic series.
  • Ganglioside amides also possess the same properties, as do the peracylated derivatives of amides, esters and simple gangliosides. All these derivatives, which are described in U.S. patent 4,713,374, can also be taken as basic substances for the new N-acylated derivatives of the present invention.
  • the basis of the present invention is the discovery that the new semisynthetic ganglioside analogues described therein and their aforesaid functional derivatives or their salts possess essentially the same pharmacological actions as natural gangliosides or their analogous functional derivatives, with a range of action which is modified in many parameters, such as speed of the "onset", duration and intensity of the sprouting phenomenon of neuronal cells, which may be regulated according to the greater or lesser lipophilic or hydrophilic character of the acyl component, or the type and entity of the side effects, which may in some cases be of a negative or positive kind according to the therapeutic problem being treated, such as above all the inhibiting activity of protein kinase C.
  • the new derivatives In many cases it is possible to use the new derivatives to exploit the particular action of acids corresponding to a given acyl group, disregarding the specific action of the ganglioside part, which in such cases acts primarily as a vehicle.
  • Such is the case, for example, of new compounds according to the invention, in which the N- and N′-acyl groups are derived from an acid which has an action on the central or peripheral nervous system, such as ⁇ -amino-butyric acid.
  • the new semisynthetic ganglioside analogues of the present invention and those which are already known and have been previously described may therefore be used in place of natural products or their already known semisynthetic derivatives and represent valuable surrogates in cases of patients who do not respond satisfactorily to treatment with conservative products or in cases which present particular idiosyncrasies or allergies. As already noted, they may be used as vehicles because of the specific pharmacological action of the acid corresponding to the acyl groups.
  • the new ganglioside analogues also possess an inhibiting action on the activation of protein kinase C which may represent an undesirable and negative effect in certain conditions of imbalance of the normal mechanisms of neurotransmitter functions.
  • This activation originates from an increased concentration of excitatory amino acids such as glutamic and/or aspartic acid; these acids, in the aforesaid abnormal conditions, have a direct toxic action on neuronal cells.
  • a major advantage of the products of the present invention which sets them apart from other protein kinase C inhibitors, such as gangliosides themselves or sphingosine, consists in their ability to prevent and inhibit the aforesaid neurotoxic action. It is important to emphasize that the products of the present invention, contrary to calcium antagonists and antagonists of glutamate receptors (particularly NMDA), only act under abnormal conditions, limiting localized neurotoxicity and maintaining neuronal plasticity, thereby allowing a more rapid recovery of impaired physiological functions.
  • the aforesaid pharmacological properties of the new semisynthetic ganglioside analogues can be illustrated by the following experiments conducted on the aforesaid N,N′-diacetyl-N,N′-di-lyso GM1 in comparison to ganglioside GM1 with regard to their capacity to protect from glutamate-induced neurotoxicity in cerebellar granule cells, where possible cytotoxic effects have also been assessed, the neuritogenic effect on neuroblastoma cells and also their capacity to reduce damage caused by ischemia in vivo.
  • EAA excitatory amino acids
  • PKC protein kinase
  • EAA excitatory amino acids
  • Glutamate (50 ⁇ M and 100 ⁇ M/Mg+2 in Locke's solution) is added to the cells and left for 15 min. at room temperature. Controls are without glutamate. The cultures are then washed 3 times with Locke's solution, the solution is removed and the cultures replaced in the original culture medium.
  • N,N′-diacetyl-N,N′-di-lyso GM1 was solubilized in Locke's solution at different concentrations (0.3 ⁇ M - 50 ⁇ M) and at different times: - pretreatment: incubated for 15 min., washed 3 times with medium containing serum and then with Locke's solution without Mg+2 before the induction of neurotoxicity; - cotreatment: incubated for 15 min. at the same time as 50 ⁇ M of glutamate.
  • Cell survival is assessed 24 hrs later by: - viable cell count by the colorimetric MTT (3-­(4,5-dimethylthiazole-2-yl)-2,5-diphenyl-tetrazolium) method; - viable cell count by the fluorimetric method: staining of the cultures for 3 min. at 22° C with a solution containing 36 ⁇ M of fluorescent diacetate (FDA) and 7 ⁇ M of propidium iodide (PI). The stained cells are immediately examined with a standard fluorescence epi-illumination microscope. Neuronal damage shortens diacetate staining and facilitates penetration of the propidium iodide (polar compound) and interaction with DNA making the complex red and fluorescent. The percentage of surviving cells is counted by measuring the acetate/propridio iodide fluorescence.
  • MTT colorimetric MTT
  • FDA fluorescent diacetate
  • PI propidium iodide
  • N2A neuroblastoma cells are seeded at a density of 10,000 cells/well (24-costar) in culture medium composed of DMEM + 10% fetal calf serum. 24 hrs after seeding the medium is substituted with 350 ⁇ l of fresh medium.
  • N,N′-diacetyl-N,N′-di-lyso GM1 and GM1 (used as positive control) are dissolved in chloroform/­methanol 2:1, dried in N2 current, resuspended in the culture medium and diluted to 50 ⁇ M or 100 ⁇ M. The cultures are fixed 24 hrs later and morphologically assessed for neuritic growth.
  • ischemia was induced in newborn rats on the 7th day of life by permanent ligature of the left carotid artery. The animals were then left to suckle their mothers for 2 hrs in order to recover. They were then placed in an hypoxic chamber (8% di O2) for 2 hrs. This results in cortical damage on the side of the occlusion, characteristically for excitatory amino acids. There is also a reduction in brain weight, and more precisely of the hemisphere on the side of the lesion.
  • N,N′-diacetyl-N,N′-di-lyso GM1 is solubilized in saline solution and administered at a dose of 10 mg/kg 1 hr before and immediately after damage.
  • the parameter considered was brain weight, taking the controlateral hemisphere as control.
  • N,N′-diacetyl-N,N′-di-lyso GM1 protects (pretreatment for 15 min.) from glutamate-induced neurotoxicity in vitro at concentrations as low as 1 ⁇ M with maximum activity (100% protection) at 3-10 ⁇ M while 0.3 ⁇ M is inactive (Fig. 1).
  • - Activity persists up to 50 ⁇ M, demonstrating intrinsic toxicity only at concentrations of >100 ⁇ M.
  • - N,N′-diacetyl-N,N′-di-lyso GM1 protects ( ⁇ 100%) from cell death induced by glutamate in vitro even when these are incubated together (cotreatment for 15 mins) (Fig. 2B).
  • N,N′-diacetyl-N,N′-di-lyso GM1 is active in inducing neuritogenesis on neuroblastoma cells to a greater degree than GM1 (Table 1).
  • - In vivo N,N′-diacetyl-N,N′-di-lyso GM1 administration reduces weight loss of the cerebral hemisphere on the side of the occlusion (Table 2).
  • the ganglioside derivative named N,N′-diacetyl-N,N′-di-lyso GM1 is able to protect from glutamate-induced neurotoxicity and to induce neuritogenesis in vitro and also to diminish brain damage following ischemia in vivo.
  • the biological activity of the new derivative can therefore be considered in those pathologies which are based on damage by glutamate, e.g., cerebral ischemia, trauma, epilepsy, chorea, Parkinson's disease, aging and dementia, cerebral disorders, hypoglycemia and hypoxia.
  • Figure 1 shows the dose-response of N,N′-diacetyl-­N,N′-di-lyso GM1 (DADL) in protecting from glutamate-­induced neurotoxicity.
  • the number of surviving cells is assessed by MTT colorimetry (3-(4,5-dimethyl-thiazole-­2-yl)-2,5 diphenyl-tetrazolium).
  • Figure 2 shows the dose-response of N,N′-diacetyl­-N,N′-di-lyso GM1 (DADL) in protecting from glutamate-­induced neurotoxicity following 15 minutes of pretreatment (Fig. 2A) and 15 minutes of cotreatment Fig. 2B). Cell survival is assessed by acetate/propidium iodide fluorimetry.
  • DADL N,N′-diacetyl­-N,N′-di-lyso GM1
  • the aforesaid semisynthetic ganglioside analogues can be used as drugs in the following pathologies: cerebral ischemia, metabolic encephalopathies such as hypoglycemia and hypoxia, encephalopathies of toxic origin, trauma, aging, epilepsy, neurodegenerative diseases such as Parkinson's disease and Huntington's chorea, and mental disorders.
  • Acids with between 1 and 11 carbon atoms from which the acyl groups of the N-acyl-lysogangliosides and N,N′-diacyl-di-lysogangliosides of the present invention are derived are saturated, with straight or branched chains, for example formic, acetic, propionic, butyric, and valerianic (valeric) acid, such as especially n-­ valerianic acid, isovalerianic acid, trimethylacetic (pivalic) acid, capronic acid and isocapronic acid, enanthic acid, caprylic acid, pelargonic acid, caprinic acid and undecylic acid, di-tert-butyl-acetic acid and 2-propyl-valerianic acid.
  • valerianic acid such as especially n-­ valerianic acid, isovalerianic acid, trimethylacetic (pivalic) acid, capronic acid and isocapronic acid, enanthic acid,
  • the longer-chained acids with a higher number of carbon atoms such as up to 24 carbons
  • the lateral chains are preferably lower alkyls with a maximum of 4 carbon atoms, especially methyl groups.
  • N,N′-diacyl-di-lysogangliosides especially those derived from the aforesaid basic gangliosides and from the acids which have received special mention.
  • N-formyl and N′-formyl-N,N′-di-lyso GM1 N-acetyl and N′-acetyl-N,N′-di-lyso GM1, N-propionyl and N′-propionyl-N,N′-di-lyso GM1, N-butyryl and N′-butyryl-N,N′-di-lyso GM1, N-pivaloyl and N′-pivaloyl-N,N′-di-lyso GM1, N-valeryl and N′-valeryl-N,N′-di-lyso GM1, N-lauroyl and N′-lauroyl-N,N′-di-lyso GM1, N-2-propylpentanoyl and N′-2-propylpentanoyl-N,N′-di-lyso GM1, N-2-propylpentanoyl
  • the invention also includes mixtures of these derivatives, such as are obtained from mixtures of acyl-lysogangliosides according to the invention, which are in turn obtained from the aforesaid ganglioside mixtures.
  • the ester groups of the new N-acyl lysoganglioside derivatives are derived particularly from alcohols of the aliphatic series and especially from those with a maximum of 12 and especially 6 carbon atoms, or of the araliphatic series with preferably one single benzene ring, optionally substituted by 1-3 lower alkyl groups (C1 ⁇ 4), for example methyl groups, and a maximum of 4 carbon atoms in the aliphatic chain, or by alcohols of the alicyclic or aliphatic alicyclic series with one single cycloaliphatic ring and a maximum of 14 carbon atoms or of the heterocyclic series with a maximum of 12 and especially 6 carbon atoms and one single hetero­cyclic ring containing a heteroatom chosen from the group formed by N, O and S.
  • the amide groups of the carboxy functions in the N-acyl lysoganglioside derivatives of the present invention are derived from ammonia or from amines of any class with preferably
  • the aforesaid alcohols and amines can be unsubstituted or substituted, especially by functions chosen from the group formed by hydroxy, amino, alkoxy groups with a maximum of 4 carbon atoms in the alkyl part, carboxy or carbalkoxy groups with a maximum of 4 atoms in the alkyl residue, alkylamino or dialkylamino groups with a maximum of 4 carbon atoms in the alkyl part, and may be saturated or unsaturated, especially with only one double bond.
  • the alcohols which are used to esterify the carboxy functions of the N-acyl lysogangliosides according to the present invention can be monovalent or polyvalent, in particular bivalent.
  • alcohols of the aliphatic series special mention should be made of lower alcohols with a maximum of 6 carbon atoms, such as methyl alcohol, ethyl alcohol, propyl and isopropyl alcohol, n-butyl alcohol, isobutyl alcohol, and tert-butyl alcohol and of the bivalent alcohols such as ethylene glycol and propylene glycol.
  • alcohols of the araliphatic series special mention should be made of those with one single benzene ring, such as benzyl alcohol and phenethyl alcohol.
  • Alcohols of the alicyclic series are preferably those with one single cycloaliphatic ring, such as cyclohexyl alcohol (cyclohexanol), terpene alcohols such as methanol and carvomenthol, or one of the terpineols or terpineneol or piperitol.
  • cyclohexyl alcohol cyclohexanol
  • terpene alcohols such as methanol and carvomenthol
  • terpineols or terpineneol or piperitol such as cyclohexyl alcohol (cyclohexanol)
  • terpene alcohols such as methanol and carvomenthol
  • the carboxy groups of the N-acyl lysogangliosides can be esterified with substituted aliphatic alcohols, for example, by amino functions, such as amino-alcohols, for example those with a maximum of 4 carbon atoms and especially amino alcohols with a dialkyl (C1 ⁇ 4)-amino group such as diethylaminoethanol.
  • amino functions such as amino-alcohols, for example those with a maximum of 4 carbon atoms and especially amino alcohols with a dialkyl (C1 ⁇ 4)-amino group such as diethylaminoethanol.
  • the carboxylamide functions according to the present invention are either derived from ammonia (the amide in this case being the unsubstituted amide -CONH2) or from primary or secondary amines, especially from those containing a maximum of 12 carbon atoms. These amines can be of an aromatic, heterocyclic, alicyclic, but especially aliphatic nature.
  • a preferred object of the present invention is represented by carboxylamide derivatives of aliphatic amines with a maximum of 12 carbon atoms, and these amines may have open, straight or branched chains and may be cyclic, such as for example alkylamines derived from alkyl groups having from 1 to 6 carbon atoms, such as methylamine or ethylamine, propylamine, hexylamine, dimethylamine, diethylamine, diisopropylamine or dihexylamine, or alkyleneamines derived from alkylene groups with straight chains having from 3 to 6 carbon atoms or corresponding chains substituted by between 1 and 3 methyl groups, such as pyrrolidine, piperidine and azepine.
  • alkylamines derived from alkyl groups having from 1 to 6 carbon atoms such as methylamine or ethylamine, propylamine, hexylamine, dimethylamine, diethylamine, diisopropyl
  • the alkyl or alkylene groups of these amines may also be interrupted in the carbon atom chain or substituted by other hetero-atoms, in particular by nitrogen atoms, and the amides of the invention are derived in this case from diamines, such as for example ethylenediamine, trimethylenediamine and piperazine.
  • the amides are amino alcohol derivatives, such as aminoethanol or aminopropanol or they are derivatives of morpholine or thiomorpholine.
  • the invention also includes derivatives, peracylated in the hydroxyls of the saccharide part, of the sialic acids and the ceramide, and of the esters and amides described herein.
  • the acyl groups in these derivatives may be derived from acids of the aliphatic, aromatic, araliphatic, alicyclic or heterocyclic series.
  • acids are formed preferably from acids of the aliphatic series with a maximum of 10 carbon atoms and especially 6 carbon atoms, for example formic, acetic, propionic, butyric, valerianic, capronic or caprinic acid. They may also be derived from acids for example with the same number of carbon atoms but substituted, particularly by hydroxyacids such as lactic acid, aminoacids such as glycine or dibasic acids such as succinic, malonic or maleic acids.
  • aromatic acids those with one single benzene nucleus should be mentioned, particularly benzoic acid and its derivatives with methyl, hydroxyl, amino or carboxy groups, such as p-aminobenzoic acid, salicylic acid or phthalic acid.
  • the invention also includes peracylated derivatives of N-acyl lysogangliosides and their aforesaid mixtures, but with free carboxy functions.
  • the acylated derivatives of the previously specified acids are also particularly important for these derivatives.
  • One important group of new derivatives is that constituted by gangliosides which are esterified or converted into amides or peracylated on the hydroxy groups, whose ester groups are derived from aliphatic alcohols with a maximum of 6 carbon atoms, saturated, unsubstituted or substituted by hydroxy or alkoxy groups with a maximum of 4 carbon atoms, amino, alkylamino or dialkylamino groups with a maximum of 4 carbon atoms in the alkyl part, carboxy groups, carbalkoxy groups with a maximum of 4 carbon atoms in the alkyl residue, and by the corresponding unsaturated alcohols with one double bond at the most, by araliphatic alcohols with one single benzene ring, unsubstituted or substituted by between 1 and 3 methyl groups, by cycloaliphatic or aliphatic-cycloaliphatic alcohols with a cyclohexane ring, unsubstituted or substituted by between 1 and 3
  • the amide groups in such derivatives are derived from ammonia or from alkylamines, dialkylamines or alkyleneamines with a maximum of 6 carbon atoms in the alkyl group and between 4 and 8 carbon atoms in the alkylene group and in which the alkyl or alkylene groups may be interrupted in the carbon atom chain by heteroatoms chosen from the group formed by nitrogen, oxygen and sulfur, the amino group being perhaps -NH in the case of the presence of a nitrogen atom substituted by an alkyl with a maximum of 4 carbon atoms and/or they may be substituted by groups chosen from the group formed by amino, alkylamino or dialkylamino groups with a maximum of 4 carbon atoms in the alkyl part or by hydroxy or alkoxy groups with a maximum of 4 carbon atoms in the alkyl group, or by araliphatic amines with one single benzene ring optionally substituted by a maximum of 3 methyl groups with a maximum of 4 carbon atoms in
  • Acyl groups which esterify the hydroxyls is such derivatives are derived from saturated or unsaturated aliphatic acids with a maximum of 6 carbon atoms, which may also be substituted by a function chosen from the group formed by hydroxy, amino and carbalkoxy groups, and their salts.
  • the sialic esters of the aforesaid new compounds derived from methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, benzyl, allyl, ethoxycarbonylmethyl and cyclohexyl alcohols, the sialic amides derived from methylamine, ethylamine, propylamine, dimethylamine, diethylamine, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, and the peracylates, perpropionylates, perbutyrylates, permaleylates, persuccinylates and peracylated analogues of the sialic esters and amides mentioned above.
  • acyl-lysogangliosides containing mainly those derived from the gangliosides GM1, GD 1a , GD 1b and GT 1b acylated with the aforesaid acids and the functional derivatives analogous to those referred to above for the derivatives of single acyl-lysogangliosides.
  • the semisynthetic ganglioside analogues of the present invention can be prepared in the known way, by acylating the di-lysogangliosides or their N-acyl or N′-acyl derivatives, or optionally by selectively deacylating the N,N′-diacyl-N,N′-­di-lysogangliosides on the sphingosine and neuraminic nitrogen.
  • Di-lysogangliosides can be obtained from gangliosides or from N-lysogangliosides by alkaline hydrolysis, for example with tetraalkylammonium hydroxides, potassium hydroxide or other alkaline compounds.
  • N-monoacyl-di-lysogangliosides can be obtained by selective acylation from di-lysogangliosides, since the sphingosine amino group is more reactive than the neuraminic amino group.
  • mildly acylating di-lysogangliosides according to the known methods for example by the acylation methods used in peptide chemistry, it is possible to obtain the aforesaid monoacyl derivatives on the sphingosine nitrogen. They are then acylated on the neuraminic nitrogen in the conventional manner.
  • the acylation procedure to obtain products according to the invention is comprised, in this case, by a two-step acylation reaction.
  • compounds having monoacyl groups on the neuraminic nitrogen can be prepared by various methods. It is possible, for example, to start with di-lysogangliosides and then effect an intermediate provisional protection of the sphingosine amino groups, which can be done for example by hydrophobic interaction with phosphatidylcholine, or by acylation with suitable protective groups, subsequent acylation on the neuraminic nitrogen with a derivative of the acid which is to be introduced into this position, and then deprotection on the sphingosine nitrogen.
  • di-lysogangliosides can be acylated on the two amino groups with the same acid and the diacyl compound can be exposed to the action of enzymes which are able to selectively break the acylamino groups alone on the sphingosine nitrogen, for example enzymes used to obtain lysogangliosides from gangliosides, such as the glycosphingolipid-ceramide-­deacylase enzyme (see plan 1).
  • N-monoacyl-N,N′-di-­lysogangliosides can however also be obtained by deacylating N,N′-diacyl-N,N′-di-lysogangliosides on the neuraminic nitrogen by selective chemical hydrolysis, for example with 0.1 molar alcoholic potassium hydrate.
  • acyl-di-lysogangliosides thus obtained it is possible, if desired, to functionally convert the carboxy groups of the sialic acids or the hydroxyls of these acids, for example to convert them into esters or amides or to convert the hydroxyls in their esterified groups with acids (peracylates).
  • N-acyl-N,N′-­di-lysogangliosides in which the acyl groups are derived from unsubstituted aliphatic acids having from 1 to 11 carbon atoms and N′-acyl-N,N′-di-lysogangliosides and N,N′-diacyl-N,N′-di-lysogangliosides, in which the acyl groups are derived from unsubstituted aliphatic acids having from 1 to 24 carbon atoms, but only 1 to 11 carbon atoms in the case of diacyl derivatives in which the N′-acyl group is acetyl (with the exception of N,N′-di-acetyl-N,N′-di-lyso GM1, N-acetyl-N,N′-di-lyso GM3, N′-acetyl-N,N′-di-lyso GM3 and N,N,N′-di
  • N-acylation according to the aforesaid procedure can be effected in the conventional manner, for example by reacting the starting products with an acylating agent, especially with a functional derivative of the acid, the residue of which is to be introduced.
  • an acylating agent especially with a functional derivative of the acid, the residue of which is to be introduced.
  • a halogen or an anhydride as the functional derivative of the acid, and the acylation is carried out preferably in the presence of a tertiary base, such as pyridine or collidine.
  • Anhydrous conditions can be used at room temperature or at higher temperatures, or the Schotten-Baumann method can also be used to advantage, operating in aqueous conditions in the presence of an organic base.
  • esters of the acids as reactive functional derivatives.
  • Enzymatic deacylation of N,N′-diacyl-N,N′-­di-lysogangliosides on the sphingosine nitrogen as previously reported can be effected under the same conditions as those used for the partial deacylation of gangliosides, for example as described in J. Biochem., 103, 1 (1988).
  • the double deacylation of N,N′-diacyl-N,N′-di-lysogangliosides to N,N′-di-­lysogangliosides can be effected in the same way as the preparation of de-N-acetyl-lysogangliosides as described for example in Biochemistry 24, 525 (1985); J. Biol. Chem. 255, 7657, (1980); Biol. Chem. Hoppe Seyler 367, 241, (1986): Carbohydr. Research 179, 393 (1988); Bioch. Bioph. Res. Comn. 147, 127 (19
  • the carboxy or hydroxy derivatives of the new acyl lysogangliosides obtained according to the aforesaid methods can be prepared according to known procedures, excluding those methods which would have the effect of altering the basic ganglioside structure, such as those involving highly acid agents or which are effected in drastically alkaline or acid conditions, or also those methods which would lead to an undesirable alkylation of the hydroxy groups in the saccharide part.
  • Esterification of the carboxy groups of N-acyl gangliosides or their conversion into amides can be done for example as described in U.S. Patent No. 4,713,374 for gangliosides.
  • Inner esters of the new derivatives can also be formed in the same way as the inner esters of gangliosides, as described for example in U.S. Patent No. 4,593,091 and in EP Patent No. 0072722.
  • These inner esters include not only compounds formed by the lactonization of sialic carboxy groups with saccharide hydroxyls, but also for example those containing lactone rings formed between the sialic carboxyls and sialic hydroxyls, since the latter are themselves bound to the saccharide part, and also other possible lactone structures.
  • the procedure of the aforesaid patents for the formation of inner esters comprises treating a ganglioside in a non-aqueous organic solvent under anhydrous conditions with a lactonizing agent.
  • Suitable organic solvents are dimethylsulfoxide, dimethylformamide, sulfolane, tetrahydrofuran, dimethoxyethane, pyridine or mixtures of these solvents.
  • Suitable lactonization reagents include carbodiimides soluble in organic solvents, such as dicyclohexylcarbodiimide, benzylisopropylcarbodiimide, benzylethylcarbodiimide, salts of 2-chloro-1-methylpyridine, ethoxyacetylene and Woodward's reagent (N-ethyl-5-phenylisoxazole-3′-sulfonate).
  • Older methods employ the reaction between a ganglioside and acetic or trichloroacetic acid or with a soluble carbodiimide in water or in an aqueous medium. All of these methods can also be used for the preparation of inner esters of the new N-acyl lysogangliosides of the invention.
  • esterification of carboxy groups that is, esterification with alcohols of the aforesaid series
  • Another esterification method comprises passing the alcohol over a resin of the type Dowex-50Wx8 (100-200 mesh form H) and treating the eluate dissolved in the same alcohol with the corresponding diazoalkane.
  • esters comprises treating a metal salt of the lysoganglioside derivative with an etherifying agent. Salts of alkaline and alkaline earth metals are used, but also any other metal salt.
  • an etherifying agent it is possible to use those mentioned in the literature, especially the esters of various inorganic acids, or organic sulfonic acids, such as hydracids, that is, in other words, hydrocarbyl halogens, such as methyl or ethyl iodide etc., or neutral sulfates or hydrocarbyl acids, sulfites, carbonates, silicates, phosphites or hydrocarbyl sulfonates, for example benzene sulfonate or methyl p-toluenesulfonate.
  • Reaction can be carried out in a suitable solvent, for example an alcohol, preferably an alcohol which corresponds to the alkyl group to be introduced, but also in nonpolar solvents, such as ketones, ethers such as dioxane or dimethylsulfoxide.
  • a suitable solvent for example an alcohol, preferably an alcohol which corresponds to the alkyl group to be introduced, but also in nonpolar solvents, such as ketones, ethers such as dioxane or dimethylsulfoxide.
  • One particularly advantageous esterification method comprises treating an inner ester of the lyso­ganglioside derivative with a mixture of the desired alcohol and its corresponding alcoholate.
  • the reaction can be carried out at a temperature corresponding to the boiling point of the alcohol, however it is also possible to operate at lower temperatures, in which case the reaction times would be longer.
  • the amides of the lysoganglioside derivatives of the present invention can be prepared by the known methods, especially the following:
  • Reaction a) can be effected directly, with or without solvent, by treating the ganglioside inner ester with ammonia or with the amine of which the amide is to be prepared.
  • the reaction can also be effected at quite low temperatures, such as from -5 to +10°, but preferably at room temperature or higher, for example between 30 and 120°C.
  • solvents it is possible to use ketones, aromatic hydrocarbons, dimethylformamide, dimethylsulfoxide, dioxane or tetrahydrofuran.
  • Reaction b) is effected preferably under the conditions described for a).
  • esters described for the present invention it is possible to use other esters, for example esters with phenols.
  • known methods already used in peptide chemistry are used, avoiding procedures which employ excessively acid or basic conditions which would lead to the disintegration of the ganglioside molecule. If the starting gangliosides are in the form of sodium salts it is advisable to first treat the salt with a Dowex-type ion exchange resin or another acid ion exchanger.
  • Acylation of the hydroxy groups of the saccharide, sialic part and optionally of the ceramide residue can also be effected in the known way, for example by acylation with a halogen or anhydride of the acid used for acylation, preferably in the presence of a tertiary base, such as pyridine or collidine.
  • a tertiary base such as pyridine or collidine.
  • the above-described peracylated derivatives are thus obtained.
  • the invention also includes modifications of the preparation procedure of the novel derivatives of the invention, wherein the procedure is interrupted at any one stage or is started from an intermediate compound and the remaining stages are carried out thereafter, or in which the starting products are formed in situ.
  • the present invention also includes pharmaceutical preparations containing as active substances one or more of the new acyl lyso-ganglioside derivatives and, in particular, those mentioned herein.
  • the pharmaceutical preparations can be formulations or compositions for oral, rectal, parenteral, local or transdermal use. They are therefore in solid or semisolid form, for example pills, tablets, jelly-like capsules, capsules, suppositories or soft gelatin capsules.
  • parenteral use it is possible to use pharmaceutical formulations designed for intramuscular, subcutaneous or transdermal administration, or suitable for infusions or intravenous injections, and it is therefore possible for the active compounds to be presented as solutions, or as freeze-dried powders to be mixed with one or more pharmaceutically acceptable excipients or diluents suitable for the aforesaid uses and with osmolarity compatible with physiological fluids.
  • preparations in the form of sprays can be considered, for example nasal sprays, creams or ointments for topical use or suitably prepared plasters for transdermal administration.
  • compositions of the invention can be used for administration to human patients or animals. They contain preferably from 0.01% to 10% by weight of active component in the case of solutions, sprays, ointments and creams and from 1% to 100% by weight and preferably from 5% to 50% by weight of active compound in the case of preparations in solid form.
  • the dosage to be administered depends on the indications in each case, on the desired effect and on the chosen administration route.
  • Another object of the present invention is represented by the therapeutic use both of the novel acyl-lysogangliosides and of those already known and listed previously. This therapeutic use concerns especially the indications discussed above.
  • the daily dosages to man by an injection route (subcutaneous or intramuscular) or a transdermal or oral route, vary from 0.05 mg to 5 mg of active substance per kg of body weight.
  • the solution is then cooled and brought to pH 6.5 with hydrochloric acid. It is left to rest for 18 hours at 4°C and then the precipitated fatty acids are eliminated by filtration. It is dialyzed against water and concentrated to 500 ml and precipitated in 5 liters of acetone.
  • N,N′-di Lyso GM1 The product is dried and high performance chromato­graphy is effected on silica gel using as eluent a mixture of chloroform/methanol/NH3 5N (55:45:10).
  • the fractions containing N,N′-di Lyso GM1 are dried and then redissolved in water. It is brought to pH 10 with NaOH 0.01 N and dialyzed, concentrated to 100 mg/ml and precipitated in 5 volumes of acetone. Yield of N,N′-di Lyso GM1: 5.7 g (70% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and 0.88 ml (6.35 mM) of triethylamine, 190 ⁇ l (3.17 mM) of formic acid and 0.4 g (1.58 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide are added at room temperature.
  • N,N′-di-formyl-N,N′-di Lyso GM1 is thus obtained: 412 mg (90% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 30 ml of chloroform/methanol/water 1:1:0.1. To the solution are added 104 ⁇ l (0.75 mM) of tri-ethylamine and 200 ⁇ l (1.80 mM) of acetic anhydride. It is left to react for 2 hrs at room temperature.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 25 ml of acetone.
  • the raw product thus obtained (475 mg) is purified by silica gel chromatography using as solvent a mixture of chloroform/ methanol/water 60:35:8.
  • N,N′-di-acetyl-N,N′-di Lyso GM1 is thus obtained: 355 mg (85.3% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide/methanol 1:1 and to this are added, at 0°C, 220 ⁇ l (1.6 mM) of triethylamine and 204 ⁇ l (1.6 mM) of propionic anhydride and it is left to react at room temperature for 168 hrs. lt is precipitated in 20 volumes of ethyl acetate, filtered and dried. The product is then purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:25:4.
  • N,N′-di-propionyl-N,N′-di Lyso GM1 is thus obtained:466 mg (82% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide/methanol 1:1 and to this are added at 0°C, 1.1 ml (7.92 mM) of triethylamine and 0.80 ml (3.96 mM) of pivalic anhydride and it is left to react at room temperature for 168 hrs. It is precipitated in 20 volumes of ethyl acetate, filtered and dried.
  • the product is then purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:25:4.
  • N,N′-di-pivaloyl-N,N′-di Lyso GM1 is thus obtained: 436 mg (77% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 0.33 ml (2.37 mM) of triethylamine, 165 ⁇ l (1.18 mM) of tert-butyl acetic acid and 0.2 g (0.79 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N,N′-di-tert-butylacetyl-N,N′-di Lyso GM1 is thus obtained: 289 mg (50% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 0.33 ml (2.37 mM) of triethylamine, 186 ⁇ l (1.18 mM) of 2-propylpentanoic acid and 0.2 g (0.79 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N,N′-di-(2-propylpentanoyl)-N,N′-di Lyso GM1 is thus obtained: 570 mg (95% theoretical).
  • N,N′-di Lyso GM1 (0.39 mM) are dissolved in 5 ml of dimethylformamide; to this solution are slowly added 145 mg (0.43 mM) of 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide (FMOC-succ.) and it is left to react for 1 hr at room temperature.
  • FMOC-succ. 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide
  • reaction When reaction is complete it is precipitated in 100 ml of acetone, filtered and dried. The product is then purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:30:6.
  • fractions containing the intermediate product N-FMOC-N,N′-di Lyso GM1 are pooled, dried and redissolved in 2.5 ml of dimethylformamide/methanol 1:1 and to this are added, at 0°C, 1.1 ml (7.92 mM) of triethylamine and 0.40 ml (3.96 mM) of methyl tri-fluoroacetate and it is left to react at room temperature for 3 days.
  • the intermediate product is dissolved in 30 ml of chloroform/methanol/water 1:1 0.1 and to this are added 250 ⁇ l (1.80 mM) of triethylamine and 100 ⁇ l (0.90 mM) of acetic anhydride. It is left to react for 2 hrs at room temperature, dried, redissolved in 5 ml of water and brought to pH 9.0 with NaOH 0.01 N. It is left at room temperature to remove the trifluoroacetyl group. It is dialyzed, concentrated to 3 ml and precipitated in 15 ml of acetone.
  • the raw product thus obtained is purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:35:8.
  • N-acetyl-N,N′-di Lyso GM1 is thus obtained: 243.8 mg (48% theoretical).
  • N,N′-di Lyso GM1 (0.39 mM) are dissolved in 5 ml of dimethylformamide; to this solution are slowly added 145 mg (0.43 mM) of 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide (FMOC-succ.) and it is left to react for 1 hr at room temperature.
  • FMOC-succ. 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide
  • reaction When the reaction is complete, it is precipitated in 100 ml of acetone, filtered and dried. The product is then purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:30:6.
  • fractions containing the intermediate product are pooled, dried and redissolved in 2.5 ml of dimethylformamide/methanol 1:1 and to this are added, at 0°C, 1.1 ml (7.92 mM) of triethylamine and 626 mg (3.96 mM) of butyric anhydride.
  • the intermediate product is dissolved in 30 ml of chloroform/methanol/water 1:1; 0.1 and to this are added 1.1 ml (7.92 ml) of triethylamine and 373 ⁇ l (3.96 mM) of acetic anhydride. It is left to react for 2 hrs at room temperature, dried, redissolved in 5 ml of Na2CO3 1 M and kept at 60°C for 1 hr. It is dialyzed, concentrated to 5 ml and precipitated in 5 volumes of acetone.
  • the raw product of the reaction is purified by silica gel chromatography using as solvent a mixture of chloroform/methanol 60:35:8.
  • N-acetyl-N′-butyrl-N,N′-di Lyso GM1 is thus obtained: 278 mg (52% theoretical).
  • N,N′-di Lyso GM1 (0.39 mM) are dissolved in 5 ml of dimethylformamide; to this solution are slowly added 145 mg (0.43 mM) of 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide (FMOC-succ.) and it is left to react for 1 hr at room temperature.
  • FMOC-succ. 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide
  • fractions containing the intermediate product are pooled, dried and redissolved in 2.5 ml of dimethylformamide/methanol 1:1 and to this are added, at 0°C, 1.1 ml (7.92 mM) of triethylamine and 1.51 g (3.96 mM) of lauric anhydride and it is left to react at room temperature for 18 hrs.
  • the intermediate product is dissolved in 30 ml of chloroform/methanol/water 1:1; 0.1 and to this are added 1.1 ml (7.92 ml) of triethylamine and 373 ⁇ l (3.96 mM) of acetic anhydride. It is left to react for 2 hours at room temperature, dried, redissolved in 5 ml of Na2CO3 1 M and kept at 60°C for 1 hr. It is dialyzed, concentrated to 5 ml and precipitated in 5 volumes of acetone.
  • the raw product of the reaction is purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:35:8.
  • N-acetyl-N′-lauroyl-N,N′-di Lyso GM1 is thus obtained: 295 mg (51% theoretical).
  • the solution is then cooled and brought to pH 6.5 with hydrochloric acid. It is left to rest for 18 hours at 4° and then the precipitated fatty acids are eliminated by filtration. It is dialyzed against water and concentrated to 500 ml and precipitated in 5 liters of acetone.
  • the product is vacuum dried and then redissolved in 100 ml of dimethylformamide.
  • the product is passed through an S-Sepharose column (H+ form) equilibrated with methanol. It is eluted with methanol, thus obtaining the N′-acetyl-N,N′- derivative of Lyso GM1 eluting with NH4Cl 10 mM in methanol.
  • the fractions containing the product are dried and then redissolved in water. The are brought to pH 10 with NaOH 0.01N and dialyzed, concentrated to 100 mg/ml and precipitated in 5 volumes of acetone. N′-acetyl-N,N′-di Lyso GM1 is thus obtained: 5 g (60% theoretical).
  • N,N′-di Lyso GM1 (0.39 mM) are dissolved in 5 ml of dimethylformamide; to this solution are slowly added 145 mg (0.43 mM) of 9-fluorenyl-methyloxy­carbonyl-N-hydroxysuccinimide dissolved in 2 ml of tetrahydrofuran and it is left to react for 1 hr at room temperature.
  • the raw product of the reaction is purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/NH3 2.5N 60:35:8.
  • the fractions containing the pure product are dried and then redissolved in 5 ml of water. It is brought to pH 10 with NaOH 0.01N and dialyzed, concentrated to 5 ml and precipitated in 5 ml of acetone.
  • N′-propionyl-N,N′-di Lyso GM1 is thus obtained: 310 mg (60.4% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 1056 ⁇ l (7.6 mM) of triethylamine, 237 ⁇ l (3.8 mM) of formic acid and 194.2 mg (0.76 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N-formyl-N′-acetyl-di Lyso GM1 is thus obtained: 391 mg (75% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 5 ml of dimethylformamide/methanol 1:1 and to this are added at 0°C, 422 ⁇ l (3.04 mM) of triethylamine and 196 ⁇ l (1.52 mM) of propionic anhydride and it is left to react at room temperature for 72 hrs. It is precipitated in 20 volumes of ethyl acetate, filtered and dried.
  • the product is then purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:35:8.
  • N-propionyl-N′-acetyl-di Lyso GM1 is thus obtained: 522 mg (70.0% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 5 ml of dimethylformamide/methanol 1:1 and to this are added at 0°C, 422 ⁇ l (3.04 mM) of triethylamine and 249 ⁇ l (1.52 mM) of butyric anhydride and it is left to react at room temperature for 72 hrs. It is precipitated in 20 volumes of ethyl acetate, filtered and dried.
  • the product is then purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:35:8.
  • N-butyryl-N′-acetyl-di Lyso GM1 is thus obtained: 527 mg (68.0% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 5 ml of dimethylformamide/methanol 1:1 and to this are added at 0°C, 528 ⁇ l (3.8 mM) of triethylamine and 780 ⁇ l (3.8 mM) of pivalic anhydride and it is left to react at room temperature for 72 hrs. It is precipitated in 20 volumes of ethyl acetate, filtered and dried.
  • the product is then purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/water 60:35:8.
  • N-pivaloyl-N′-acetyl-di Lyso GM1 is thus obtained: 490 mg (94.0% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 316 ⁇ l (2.28 mM) of triethylamine, 143 ⁇ l (1.14 mM) of hexanoic acid and 194.2 mg (0.76 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N-hexanoyl-N′-acetyl-di Lyso GM1 is thus obtained: 392 mg (73% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 1056 ⁇ l (7.6 mM) of triethylamine, 595 ⁇ l (3.8 mM) of 2-propyl-pentanoic acid and 194.2 mg (0.76 mM) of chloro-methylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N-(2-propylpentanoyl)-N′-acetyl-di Lyso GM1 is thus obtained: 428 mg (75% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 316 ⁇ l (2.28 mM) of triethylamine, 181 ⁇ l (1.14 mM) of octanoic acid and 194.2 mg (0.76 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N-octanoyl-N′-acetyl-di Lyso GM1 is thus obtained: 427 mg (78% theoretical).
  • N′-acetyl-N,N′-di Lyso GM1 500 mg (0.38 mM) of N′-acetyl-N,N′-di Lyso GM1 are dissolved in 2.5 ml of dimethylformamide and to this are added at room temperature 316 ⁇ l (2.28 mM) of triethylamine, 152 mg (1.14 mM) of lauric acid and 194.2 mg (0.76 mM) of chloromethylpyridinium iodide dissolved in 2.5 ml of dimethylformamide.
  • N-lauroyl-N′-acetyl-di Lyso GM1 is thus obtained: 353 mg (62% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 5 ml of dimethylformamide and to this are added 1 ml of Triton X 100 and 104 ⁇ l (0.75 mM) of tri-ethylamine. This is stirred until a clear solution is obtained.
  • Reaction is conducted for 24 hrs at room temperature after which the solution is concentrated to 5 ml and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:30:6.
  • the product is then purified by further silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:35:8.
  • the pure fractions are pooled, evaporated, treated with Na2CO3 1N, dialyzed against distilled H2O, concentrated to 5 ml and precipitated in 100 ml of acetone.
  • N-decanoyl-N′-acetyl-di Lyso GM1 is thus obtained: 184 mg (32% theoretical).
  • N,N′-di Lyso GM1 500 mg (0.39 mM) of N,N′-di Lyso GM1 are dissolved in 5 ml of dimethylformamide and to this are added 1 ml of Triton X 100 and 104 ⁇ l (0.75 mM) of tri-ethylamine. This is stirred until a clear solution is obtained.
  • Reaction is conducted for 24 hrs at room temperature after which the solution is concentrated to 5 ml and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:30:6.
  • the product is then purified by further silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:35:8.
  • the pure fractions are pooled, evaporated, treated with Na2CO3 1N, dialyzed against distilled H2O, concentrated to 5 ml and precipitated in 100 ml of acetone.
  • GM1 500 mg (0.31 mM) of GM1 are dissolved in 50 ml of sodium hydrate 1N. The reaction mixture is then kept at a temperature of 90°C for 18 hrs. The solution thus obtained is dialyzed, concentrated to 2.5 ml and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by silica gel chromatography using as eluent a mixture of chloroform/methanol/H2O 60:30:6.
  • Natural N′-lyso GM1 is thus obtained: 350 mg (72% theoretical).
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 80 mM and 750 mg (1.7 mM) of myristic anhydride.
  • the condensation reaction is carried out at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • Natural N′-myristoyl-N′-lyso GM1 is thus obtained: 500 mg (87.8% theoretical).
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 80 mM and 900 mg (1.82 mM) of palmitic anhydride.
  • the condensation reaction is carried out at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 80 mM and 100 mg (1.81 mM) of stearic anhydride dissolved in 20 ml of tetrahydrofuran.
  • the condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.75 ml (0.54 mM) of triethylamine and 0.75 ml (6.75 mM) of pivalic anhydride.
  • the condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/­methanol/water 60:20:3.
  • Natural N′-pivaloyl-N′-lyso GM1 is thus obtained: 440 mg (83.3% theoretical).
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 50 mM and 0.25 ml (1.95 mM) of propionic anhydride.
  • the condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by silica gel preparative chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 50 mM and 0.25 ml (1.53 mM) of n-butyric anhydride.
  • the condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by silica gel preparative chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • Natural N′-butyryl-N′-lyso GM1 is thus obtained: 450 mg (85.9% theoretical).
  • the condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • N′-lyso GM1 500 mg (0.33 mM) of natural N′-lyso GM1 are dissolved in 50 ml of chloroform/methanol 1:1 and to this solution are added 0.5 ml of acetate buffer pH 5.7, 50 mM and 600 mg (1057 mM) of lauric anhydride. The condensation reaction is conducted at 25°C for 18 hrs under constant stirring.
  • the product is dried, gathered with 5 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • the raw product thus obtained is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 60:20:3.
  • N-pivaloyl-N′-acetyl-di Lyso GM1 5 g (3.1 mM) of N-pivaloyl-N′-acetyl-di Lyso GM1 are dissolved in 50 ml of N-methylpyrrolidone and to this solution are added 0.95 g (3.72 mM) of 2-chloro-1-methylpyridinium iodide and 0.52 ml (3.72 mM) of triethylamine under constant stirring.
  • Reaction is conducted for 18 hours at 4°C, after which the solution is filtered and precipitated in 500 ml of acetone.
  • the raw product thus obtained (4.7 g) is gathered with 25 ml of chloroform/isopropanol 1:1, filtered, precipitated in 125 ml of acetone and vacuum-dried.
  • the mixture is neutralized with anhydrous Dowex AG 50x8 resin, H+ form, the resin is separated by filtration and washed with ethanol/methylene chloride 1:1 and the solution is then dried. The residue is gathered with 50 ml of methylene chloride/ethanol 1:1 and the product is precipitated with 250 ml of acetone.
  • the raw product thus obtained (4.9 g) is purified by preparative chromatography with Merck silica gel, using as solvent a mixture of chloroform/methanol/isopropanol/­ammonium carbonate 2% 1140:620:180:140.
  • the pure fractions are pooled, evaporated to dryness, and redissolved in 15 ml of chloroform/methanol 1:1, and the product is precipitated with 75 ml of acetone.
  • the raw product thus obtained (4.9 g) is purified by medium pressure preparative chromatography (12 atm) with Merck silica gel, using as solvent a mixture of chloroform/methanol/isopropanol/ammonium carbonate 2% 1140:620:180:140.
  • the pure fractions are pooled, evaporated to dryness, and redissolved in 15 ml of chloroform/methanol 1:1, and the product is precipitated with 75 ml of acetone.
  • the raw product thus obtained (4.9 g) is purified by medium pressure preparative chromatography (12 atm) with Merck silica gel, using as solvent a mixture of chloroform/methanol/isopropanol/ammonium carbonate 2% 1140:620:180:140.
  • the pure fractions are pooled, evaporated to dryness, and redissolved in 15 ml of chloroform/methanol 1:1, and the product is precipitated with 75 ml of acetone.
  • the solution is partitioned with n-butanol/water 2:1 to eliminate the DMSO and salts.
  • the butanol solution is evaporated, the residue gathered with 50 ml of chloroform/benzyl alcohol 1:1 and the product of the reaction is precipitated with 250 ml of acetone.
  • the raw product thus obtained (5.3 g) is purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 65:32:7.
  • the pure fractions are pooled, evaporated, and redissolved in 15 ml of chloroform/isopropanol 1:1, and the product is precipitated with 75 ml of acetone.
  • the raw product thus obtained (4.8 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified by silica gel preparative chromatography using as first solvent a mixture of chloroform/methanol/ water 60:40:9 and as second solvent a mixture of chloroform/methanol/water 55:45:10.
  • the pure fractions, eluted and pooled are evaporated, and dissolved in 15 ml of chloroform/methanol 1:1, and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (4.9 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residue ester groups, dialyzed in water, vacuum-dried and then purified by preparative chromatography with Sephadex DEAE A25, acetate form, using as solvent a mixture of chloroform/ methanol/water 30:60:8.
  • the pooled neutral fractions are evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (4.8 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified by preparative chromatography on a silica gel column using as solvent a mixture of chloroform/methanol/ammonia 25N 60:40:9.
  • the pure fractions, eluted and pooled, are evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the product precipitated with 75 ml of acetone.
  • the raw product thus obtained (5.2 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified by preparative silica gel chromatography using as solvent a mixture of chloroform/methanol/water 110:40:6.
  • the pure fractions are eluted, pooled, evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (5.2 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified using as first solvent a mixture of chloroform/methanol/ammonia 2.5 N 60:40:9 and as second solvent chloroform/methanol/water 60:40:9.
  • the pure, eluted fractions are pooled, evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (5.1 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified using as first solvent a mixture of chloroform/methanol/ammonia 2.5 N 60:40:9 and as second solvent chloroform/methanol/water 60:40:9.
  • the pure, eluted fractions are pooled, evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (5.1 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified using as first solvent a mixture of chloroform/methanol/ammonia 2.5 N 60:40:9 and as second solvent chloroform/methanol/water 60:40:9.
  • the pure, eluted fractions are pooled, evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • the raw product thus obtained (5.1 g) is treated with 100 ml of Na2CO3 1% for 30 minutes at 25°C to hydrolyze the residual ester groups, dialyzed in water, vacuum-dried and then purified by preparative chromatography with Sephadex DEAE A25, acetate form, using as solvent a mixture of chloroform/methanol/water 30.60.8.
  • the pooled neutral fractions are evaporated, dissolved in 15 ml of chloroform/methanol 1:1 and the amide precipitated with 75 ml of acetone.
  • Bovine brain tissue extracted from the animal, is homogenized in phosphate buffer at pH 6.8. 6 volumes of tetrahydrofuran are then added and the resulting mixture is centrifuged. The upper layer is extracted twice with tetrahydrofuran. After centrifugation the non-polar materials are removed by partitioning with ethyl ether and the aqueous tetrahydrofuran phase is introduced into an ion exchange column equilibrated with 50% ethanol. Barium hydroxide and four volumes of ice-cold ethanol are added to the effluent from the column. After refrigeration for 18 hours a precipitate is gathered which is then lightly acidified with hydrochloric acid dissolved in water.
  • the solution thus obtained is dialyzed and freeze-dried.
  • the yield at this point is approximately 0.6 mg of raw ganglioside mixture per gram of nervous tissue used.
  • the freeze-dried powder is dispersed in 20 volumes of chloroform-methanol 2:1, the solution obtained is filtered until completely clear, and then partitioned adding 0.2 volumes of a solution of potassium chloride in water at 0.88%.
  • the upper layer is separated, dialyzed and freeze-­dried.
  • the final yield is approximately 0.3 mg of a purified mixture of ganglioside salts per gram of brain tissue.
  • the ganglioside mixture obtained can be fractioned into various portions representing substantially pure gangliosides (in the sense used in the general description), using silicic acid columns and eluting with mixtures of methanol-chloroform. On average, the following composition was thus obtained: 40% of ganglioside GD1a, 21% of ganglioside GM1, 19% of ganglioside GT1b and 16% of ganglioside GD1b.
  • the intermediate reaction product thus obtained is redissolved in 500 ml of chloroform/methanol/water 1:1:0.1. To this solution are added 2.08 ml (15 mM) of triethylamine and 1.4 ml (15 mM) of acetic anhydride. It is left to react for 2 hrs at room temperature.At the end of reaction it is dried, gathered with 10 ml of chloroform/methanol 1:1 and precipitated in 100 ml of acetone.
  • one 2 ml vial contains: - active substance mg 5 - sodium chloride mg 16 - citrate buffer pH 6 in distilled water to make ml 2
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 4, 13 and 14.
  • one 2 ml vial contains: - active substance mg 50 - sodium chloride mg 16 - citrate buffer pH 6 in distilled water to make ml 2
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 9, 16, 23, 28, 29 and 30.
  • one 4 ml flacon contains: - active substance mg 100 - sodium chloride mg 32 - citrate buffer pH 6 in distilled water to make ml 4
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 5, 6, 15 and 27.
  • Preparation Nos. 1, 2 and 3 can be administered directly to animals or humans by any one of the described routes. Furthermore, the compounds can contain other pharmaceutically active substances.
  • the preparations illustrated in this Example are presented in twin flacons.
  • the first flacon contains the active substance in the form of a freeze-dried powder in quantities varying between 10% and 90% in weight together with a pharmaceutically acceptable excipient, with glycine or mannitol.
  • the second flacon contains the solvent, as a solution of sodium chloride and a citrate buffer.
  • the pharmaceutical form where the freeze-dried powder of the active substance is contained in a flacon is the preferred form of the present invention.
  • one 2 ml flacon of freeze-dried powder contains: - active substance mg 5 - glycine mg 30 b.
  • one 2 ml vial of solvent contains: - sodium chloride mg 16 - citrate buffer in distilled water to make ml 2
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 32 and 33.
  • one 3 ml vial of freeze-dried powder contains: - active substance mg 5 - mannitol mg 40 b.
  • one 2 ml vial of solvent contains: - sodium chloride mg 16 - citrate buffer in distilled water to make ml 2
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 32 and 33.
  • one 3 ml vial of freeze-dried powder contains: - active substance mg 50 - glycine mg 25 b.
  • one 3 ml vial of solvent contains: - sodium chloride mg 24 - citrate buffer in distilled water to make ml 3
  • the active substance is chosen from the group formed by the ganglioside derivatives described in Examples 34 and 36.
  • one 3 ml vial of freeze-dried powder contains: - active substance mg 50 - mannitol mg 20 b.
  • one 3 ml vial of solvent contains: - sodium chloride mg 24 - citrate buffer in distilled water to make ml 3
  • the active substance is chosen from the group formed by the ganglioside derivatives described in Examples 34 and 36.
  • one 5 ml flacon of freeze-dried powder contains: - active substance mg 150 - glycine mg 50 b.
  • one 4 ml vial of solvent contains: - sodium chloride mg 32 - citrate buffer in distilled water to make ml 4
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 44 and 45.
  • one 5 ml flacon of freeze-dried powder contains: - active substance mg 100 - mannitol mg 40 b.
  • one 4 ml vial of solvent contains: - sodium chloride mg 32 - citrate buffer in distilled water to make ml 4
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 44 and 45.
  • one 3 ml flacon contains: - sterile, micronized active substance mg 40 b.
  • one 3 ml vial of solvent contains: - Tween 80 mg 10 - sodium chloride mg 24 - phosphate buffer in distilled water to ml 3
  • the active substance is chosen from the group formed by the ganglioside derivatives described in Examples 37 and 38.
  • one 5 ml flacon contains: - sterile, micronized active substance mg 100
  • one 4 ml vial of solvent contains: - Tween 80 mg 5 - soybean lecithin mg 5 - sodium chloride mg 36 - citrate buffer in distilled water to make ml 4
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 40 and 42.
  • one plaster contains: - active substance mg 100 - glycerin g 1.6 - polyvinyl alcohol mg 200 - polyvinylpyrrolidone mg 100 - excipient to aid transdermal penetration mg 20 - water g 1.5
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 32, 33 and 34.
  • ointment 100 gr contain: - active substance (in 5 gr of mixed phospholipid liposomes) g 4.0 - polyethylene glycol monostearate g 1.5 - glycerin g 1.5 - p-hydroxybenzoic acid ester mg 125 - water g 72.9
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 32, 33 and 34.
  • one tablet contains: - active substance mg 20 - microcrystalline cellulose mg 150 - lactose mg 20 - amide mg 10 - magnesium stearate mg 5
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 1, 2, 3, 8 and 11.
  • one tablet contains: - active substance mg 30 - carboxymethyl cellulose mg 150 - amide mg 15 - shellac mg 10 - sucrose mg 35 - coloring mg 0.5
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 13 and 23.
  • one gelatinous capsule contains: - active substance mg 40 - lactose mg 100 - gastroresistant coating mg 5
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 35, 41 and 47.
  • one soft gelatin capsule contains: - active substance mg 50 - vegetable oil mg 200 - beeswax mg 20 - gelatin mg 150 - glycerin mg 50 - coloring mg 3
  • the active substance is chosen from the group formed by the ganglioside derivatives described in any one of Examples 35, 41 and 47.

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WO1993003049A1 (fr) * 1991-08-01 1993-02-18 Fidia S.P.A. Nouveaux derives de gangliosides
WO1993016089A1 (fr) * 1992-02-14 1993-08-19 Werner Reutter Glycosphingolipides, procede pour leur fabrication et agents pharmaceutiques les contenant
EP2410846A1 (fr) * 2009-03-25 2012-02-01 Seneb Biosciences, Inc. Glycolipides en tant que traitement de maladies

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IT1232176B (it) * 1989-07-27 1992-01-25 Fidia Farmaceutici Derivati di-lisogangliosidi
IT1239060B (it) * 1990-05-04 1993-09-20 Fidia Spa Processo per la modulazione selettiva dell'espressione e della funzione di un determinante sulla superficie cellulare attraverso appropriati agenti chimici
NZ531139A (en) 2001-08-29 2007-09-28 Neose Technologies Inc Synthetic ganglioside derivatives and compositions thereof
US7888331B2 (en) 2003-03-06 2011-02-15 Seneb Biosciences, Inc. Ganglioside compositions and methods of use
KR20180064493A (ko) 2015-10-09 2018-06-14 텐사 코포레이션, 엘엘씨 공압출된 다층 폴리머로 제조된 지오그리드

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0167449A2 (fr) * 1984-07-03 1986-01-08 FIDIA S.p.A. Dérivés de gangliosides
EP0315113A2 (fr) * 1987-11-02 1989-05-10 FIDIA S.p.A. Esters internes de gangliosides ayant une activité analgésique-antiinflammatoire
EP0328420A2 (fr) * 1988-02-12 1989-08-16 The Biomembrane Institute Gangliosides contenant l'acide de-N-acétylsiatique et leur utilisation comme modificateurs de la physiologie des cellules
EP0373039A2 (fr) * 1988-12-02 1990-06-13 FIDIA S.p.A. Dérivés de lysogangliosides

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4476119A (en) * 1981-08-04 1984-10-09 Fidia S.P.A. Method for preparing ganglioside derivatives and use thereof in pharmaceutical compositions
US4716223A (en) * 1981-08-04 1987-12-29 Fidia, S.P.A. Method for preparing ganglioside derivatives and use thereof in pharmaceutical compositions
US4593091A (en) * 1981-08-04 1986-06-03 Fidia, S.P.A. Method for preparing ganglioside derivatives and use thereof in pharmaceutical compositions
JPH06795B2 (ja) * 1985-04-02 1994-01-05 理化学研究所 アシアロガングリオシド関連化合物の製造方法
DE3852526D1 (de) * 1987-06-26 1995-02-02 Solco Basel Ag Neue pharmazeutische Präparate sowie neue Lactosylverbindungen und ihre Herstellung.
IT1253832B (it) * 1991-08-01 1995-08-29 Fidia Spa Derivati di gangliosidi

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0167449A2 (fr) * 1984-07-03 1986-01-08 FIDIA S.p.A. Dérivés de gangliosides
EP0315113A2 (fr) * 1987-11-02 1989-05-10 FIDIA S.p.A. Esters internes de gangliosides ayant une activité analgésique-antiinflammatoire
EP0328420A2 (fr) * 1988-02-12 1989-08-16 The Biomembrane Institute Gangliosides contenant l'acide de-N-acétylsiatique et leur utilisation comme modificateurs de la physiologie des cellules
EP0373039A2 (fr) * 1988-12-02 1990-06-13 FIDIA S.p.A. Dérivés de lysogangliosides

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF BIOCHEMISTRY vol. 103, no. 1, January 1988, TOKYO JP pages 1 - 4 HIRABAYASHI Y. ET AL 'A Novel Glycosphingolipid Hydrolyzing Enzyme, Glycosphingolipid Ceramide Deacylase, which cleaves the linkage between the Fatty Acid and Sphingosine Base in Glyosphingolipids' *
JOURNAL OF LIPID RESEARCH vol. 26, no. 2, 1985, pages 248 - 257 SONNINO S. ET AL 'Preparation of GM1 ganglioside, molecular species having homogeneous fatty acid and long chain base moieties' *
METHODS IN ENZYMOLOGY vol. 179, no. F, 1989, SAN DIEGO US pages 242 - 253 NORES G.A. ET AL 'Synthesis and Characterization of Ganglioside GM3 Derivatives: Lyso-GM3, De-N-acetyl-GM3,a dn Other Compounds' *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993003049A1 (fr) * 1991-08-01 1993-02-18 Fidia S.P.A. Nouveaux derives de gangliosides
US5350841A (en) * 1991-08-01 1994-09-27 Fidia S.P.A. Ganglioside derivatives
WO1993016089A1 (fr) * 1992-02-14 1993-08-19 Werner Reutter Glycosphingolipides, procede pour leur fabrication et agents pharmaceutiques les contenant
EP2410846A1 (fr) * 2009-03-25 2012-02-01 Seneb Biosciences, Inc. Glycolipides en tant que traitement de maladies
EP2410846A4 (fr) * 2009-03-25 2012-08-29 Seneb Biosciences Inc Glycolipides en tant que traitement de maladies
EP3175857A1 (fr) * 2009-03-25 2017-06-07 Seneb Biosciences Inc. Glycolipides en tant que traitement de maladies
US10555959B2 (en) 2009-03-25 2020-02-11 La Jolla Pharmaceutical Company Glycolipids as treatment for disease

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NZ234649A (en) 1992-01-29
IT1232175B (it) 1992-01-25
PL165209B1 (pl) 1994-11-30
JPH0358995A (ja) 1991-03-14
HU210923B (en) 1995-09-28
DE69031448T2 (de) 1998-02-26
AU5982990A (en) 1991-01-31
ATE158297T1 (de) 1997-10-15
HUT54173A (en) 1991-01-28
US5484775A (en) 1996-01-16
CA2022138A1 (fr) 1991-01-28
HU904640D0 (en) 1991-01-28
FI903753A0 (fi) 1990-07-27
ES2106025T3 (es) 1997-11-01
PL286249A1 (en) 1991-08-26
EP0410881B1 (fr) 1997-09-17
NO903333L (no) 1991-01-28
IT8948246A0 (it) 1989-07-27
KR910002887A (ko) 1991-02-26
IL95169A0 (en) 1991-06-10
EP0410881A3 (en) 1993-01-20
DE69031448D1 (de) 1997-10-23
NO903333D0 (no) 1990-07-26

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